1. Physical Chemistry

1.1 Atomic Structure

1.1.1 Structure of the Atom

1.1.2 Isotopes

1.1.3 Relative Mass

1.1.4 Mass Spectrometry

1.2 Ions & Electrons

1.2.1 Ionisation Energy

1.2.2 Quantum Shells

1.2.4 Electronic Configurations

1.3 The Periodic Table

1.3.1 Periodicity

1.4 Bonding

1.4.1 Ionic Bonding Overview

1.4.2 Representing Ionic Bonding

1.4.3 Ionic Trends

1.4.4 Physical Properties of Ionic Compounds

1.4.5 Covalent Bonding Overview

1.4.6 Covalent Dot-and-Cross Diagrams

1.4.7 Bond Length & Bond Strength

1.4.8 Shapes of Covalent Compounds

1.5 Structure

1.5.1 Electronegativity

1.5.2 Intermolecular Forces

1.5.3 Hydrogen Bonding

1.5.4 Intermolecular Forces & Physical Properties

1.5.5 Metallic Bonding

1.5.6 Giant Lattices

1.5.7 Covalent Structures

1.5.8 Predicting Structures

1.6 Formulae, Equations & Avogadro

1.6.1 Empirical & Molecular Formulae

1.6.2 Balanced Equations

1.6.3 Applying Equations

1.6.4 The Mole & the Avogadro Constant

1.6.5 Amount of Substance Calculations

1.7 Reaction Calculations

1.7.1 Reacting Volume Calculations

1.7.2 Titrations

1.7.3 Error & Uncertainty

1.7.4 Yield & Atom Economy

1.8 Energetics I

1.8.1 Enthalpy Changes

1.8.3 Calorimetry

1.8.4 Hess Cycles

1.8.5 Bond Enthalpy

Enthalpy Level Diagrams

1.9 Kinetics

1.9.1 Collision Theory & Rates

1.9.2 Calculating Rates of Reaction

1.9.3 Maxwell-Boltzmann Distributions

1.9.4 Catalysts in Industry

1.10 Equilibrium I

1.10.1 Dynamic Equilbrium

1.10.2 Le Chatelier's Principle

1.10.3 The Rate & Yield Compromise

1.10.4 Deducing Kc Expressions

2. Inorganic Chemistry

2.1 Redox I

2.1.1 Oxidation Number

2.1.2 Types of Reduction & Oxidation

2.1.3 Redox & Disproportionation

2.1.4 Ionic Equations

2.2 Groups 1 & 2

2.2.1 Explaining Group 2 Trends

2.2.2 Reactions of Group 2

2.2.3 Group 2 Hydroxides & Sulfates

2.2.4 Group 1 & 2 Carbonates & Nitrates

2.2.5 Flame Tests

2.3 Group 7

2.3.1 Group 7 Trends

2.3.2 Halogen Displacement Reactions

2.3.3 Halogen Redox Reactions

2.3.4 Halide Ion Reactions

3. Organic Chemistry

3.1 Introduction to Organic Chemistry

3.1.1 formulae of organic compounds

3.1.2 Homologous Series and Functional Groups

3.1.3 Nomenclature and Classification

3.1.4 Structural Isomerism

3.1.5 Stereoisomerism

3.2 Alkanes

3.2.1 Describing Alkanes

3.2.2 Alkane Fuels

3.2.3 Pollution from Combustion

3.2.4 Reducing Pollution

3.2.5 Free Radicals

3.3 Alkenes

3.3.1 Describing Alkenes

3.3.2 Bonding in Alkenes

3.3.3 Electrophilic addition

3.3.4 Electrophilic Addition Mechanism

3.3.5 Saturation Test

3.3.6 Addition Polymerisation

3.3.7 Waste Polymers

3.4 Halogenoalkanes

3.4.1 Classifying Halogenoalkanes

3.4.2 Nucleophilic Substitution

3.4.3 Nucleophilic Substitution Mechanism

3.4.4 Hydrolysis of Halogenoalkanes

3.4.5 Reactivity of Halogenoalkanes

3.5 Alcohols

3.5.1 Classifying Alcohols

3.5.2 Reactions of Alcohols

3.5.3 Organic Liquid Preparation & Purification

3.6 Modern Analytical Techniques I

3.6.1 Mass Spectrometry

3.6.2 Infrared (IR) Spectroscopy

4. Core Chemistry Practicals

4.1 Physical Chemistry Core Practicals

4.1.1 Molar Volume of a Gas

4.1.2 Standard Solutions

4.1.3 Determining Concentrations

4.1.4 Determining Enthalpy Change of Reaction

4.2 Inorganic & Organic Chemistry Core Practicals

4.2.1 Hydrolysis of Halogenoalkanes

4.2.2 Ethanol Oxidation

4.2.3 Chlorination of 2-Methylpropan-2-ol

4.2.4 Qualitative Analysis